The Recall Desk

State

Ohio product recalls

72,969 recalls have nationwide distribution and so reach Ohio. 11,723 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,723
Critical
2,107
Severe
2,413
Most recent
2026-09-16

Of the 11,723 recalls naming Ohio we have scored against our rubric, 2,107 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,413 (21%) are Severe.

Which agencies issued them

These figures cover only the 11,723 recalls whose distribution notice names Ohio specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6201–6225 of 84692

  • HighFDA (Devices)·Z-2151-2025·2025-07-30

    Nellcor bedside SpO2 monitor alarms may not be heard or recognized

    The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.

    Product
    Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2025·2025-07-30

    HSG procedure trays label non-sterile iodine pouches as sterile

    HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.

    Product
    HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterography procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2136-2025·2025-07-30

    Endosee system convenience trays label non-sterile iodine pouches as sterile

    Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.

    Product
    Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0541-2025·2025-07-30

    Budesonide inhalation ampoules recalled after leakage and empty ampoule complaint

    Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.

    Product
    BUDESONIDE — BUDESONIDE (BUDESONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0535-2025·2025-07-30

    Compounded epinephrine lidocaine vials returned subpotent assay results in stability testing

    Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.

    Product
    Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0325-2025·2025-07-30

    Ritz cracker sandwich variety packs recalled over undeclared peanut from mispackaging

    Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.

    Product
    Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38 oz Packs) Net Wt. 27.3 oz (20-1.38 oz packet of cracker sandwiches inside cartons of varying sizes). 20-27.3 OZ (Case: 6 - 27.3 Oz Cartons in master carton. UP
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-2134-2025·2025-07-30

    Azurion 7 M20 C-arm gearbox mounting bolts may become loose

    The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.

    Product
    Azurion 7 M20. Fluoroscopic X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2137-2025·2025-07-30

    Endosee convenience kits label non-sterile iodine pouches as sterile

    Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.

    Product
    Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0311-2025·2025-07-30

    Turkeyfoot Creek Creamery cookies and cream ice cream has undeclared allergens

    Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0309-2025·2025-07-30

    Turkeyfoot Creek Creamery chocolate peanut butter ice cream has undeclared soy

    Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0323-2025·2025-07-30

    Ritz peanut butter cracker 20 count cartons recalled over undeclared peanut

    Ritz Peanut Butter Cracker Sandwiches in 27.6 oz 20 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 24,446 cases are affected.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside cartons. And 6x20(6 - 27.6 oz Cartons) in master carton. UPC 1 00 44000 07584 2
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·H-0319-2025·2025-07-30

    Artisan style half loaves recalled over undeclared hazelnut from mispackaging

    Artisan Style 1/2 Loaf white bread is being recalled because product containing hazelnuts was put in bags whose allergen statement does not include hazelnuts. 883 loaves are affected.

    Product
    Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two splits on top 7/13/2025 - Best By Flexible plastic bag
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·H-0324-2025·2025-07-30

    Ritz peanut butter cracker 40 count cartons recalled over undeclared peanut

    Ritz Peanut Butter Cracker Sandwiches in 55.2 oz 40 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 224 cases are affected.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton. 40 - 55.2oz Cartons in master carton. UPC 0 44000 07819 5
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-2168-2025·2025-07-30

    SmartSync Patient Connector limited the window to abort high voltage therapy

    The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.

    Product
    Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2132-2025·2025-07-30

    Discovery MR750w gradient coils can produce acoustic noise above the limit

    GE HealthCare Discovery MR750w 3.0T MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    Discovery MR750w 3.0T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0312-2025·2025-07-30

    Turkeyfoot Creek Creamery cookie dough ice cream has undeclared soy and wheat

    Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2133-2025·2025-07-30

    SIGNA PET/MR gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA PET/MR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0315-2025·2025-07-30

    Turkeyfoot Creek Creamery cacao strawberry ice cream has undeclared soy

    Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0308-2025·2025-07-30

    Turkeyfoot Creek Creamery Avalanche ice cream has undeclared soy and wheat

    Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0326-2025·2025-07-30

    Ritz peanut butter cracker sandwiches recalled over undeclared peanut from mispackaging

    Ritz Peanut Butter Cracker Sandwiches are being recalled because of undeclared peanut allergens due to mispackaging. 37,985 units are affected across nearly every state.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 14X8-Case: 14 - 11.04 Oz Cartons in master carton. UPC 0 44000 88210 5
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-2171-2025·2025-07-30

    Stryker StrykeFlow irrigator with tip may leak solution into handpiece

    The Stryker StrykeFlow Disposable Suction/Irrigator with Disposable Tip is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.

    Product
    Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0310-2025·2025-07-30

    Turkeyfoot Creek Creamery brownie ice cream has undeclared soy and wheat

    Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2163-2025·2025-07-30

    ACUVUE OASYS MAX multifocal daily lenses have bubbles and voids

    ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.

    Product
    ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
    Category
    Medical Device
    Distribution
    Distributed nationwide